Senior Clinical Research Associate
Senior Clinical Research Associate
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Job Description
Job Description
If you:
Join a multiawardwinning leading biopharmaceutical company
Be part of growing team of Clinical Research Associates
Use new technology and smart monitoring tools
Have flexibility of work and good worklife balance
Apply today!
On this position you will be accountable for performance and compliance for assigned protocols and sites in a country. You will act as primary site contact and site manager throughout all phases of a clinical research study taking overall responsibility of allocated sites and actively develop and expand the territory for clinical research finding and developing new sites.
Your key responsibilities:
Conduct site visits (validation visits initiation visits monitoring visits closeout visits) and record clear comprehensive and accurate visit & nonvisit contact reports.
Ensure by monitoring activities that:
Data generated at site are complete accurate and unbiased.
Subjects right safety and wellbeing are protected.
Perform clinical study site management/monitoring activities in compliance with local regulations ICHGCP Sponsor SOPs protocol Site Monitoring Plan and associated documents.
Coordinate and manage various tasks in collaboration with other sponsor roles.
Communicate with Investigators and site staff on issues related to protocol conduct recruitment retention protocol deviations regulatory documentation site audits/inspections and overall site performance.
Identify and assess site performance quality or compliance problems in collaboration with CRA Manager Project Manager Therapeutical Area Head and Country Director as needed.
Manage and maintain clinical trial systems such as CTMS eTMF etc.
Share the knowledge and best practices nurture a learning culture to boost efficiency and competence of our team.
Follow the country strategy defined by Country Director.
You should apply if you have:
Min. 3 years of direct site management (monitoring) experience in a bio/pharma/CRO.
Proven skills in site management including management of site performance and patient recruitment.
Good IT skills ability to learn and operate new IT applications.
Ability to understand and analyse data/metrics.
Capable of managing complex issues works in a solutionoriented manner.
Fluent in English (verbal and written) and local language excellent communication and presentation skills.
Good understanding and working knowledge of clinical research local regulations ICHGCP.
M.A/ degree with strong emphasis in medical/bioscience background.
Ability to travel domestically and internationally approximately 50% of working time. Expected travelling 23 days/week.
Valid driving license.
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no preexisting agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.
Employee Status:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
RemoteShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
05/8/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
Senior IC
Employment Type
Full-Time
